Tanaka M.Thoumrungroj A.Sutthiphong T.Longchin P.Hunsom M.Mahidol University2025-09-292025-09-292025-12-20Colloids and Surfaces A Physicochemical and Engineering Aspects Vol.727 (2025)09277757https://repository.li.mahidol.ac.th/handle/123456789/112345A high-surface-area mesoporous TiO<inf>2</inf> photocatalyst was synthesized through a sequential hydrothermal-calcination process for the photocatalytic recovery of silver from industrial cyanide-based plating effluent. Preliminary results indicated that TiO<inf>2</inf> synthesized at low calcination temperatures (e.g., < 500 °C) exhibited low crystallinity, high BET surface area, an anatase-brookite mixed phase, and high bandgap values. In contrast, TiO<inf>2</inf> synthesized at higher temperatures (650 – 700 °C) showed high crystallinity, low BET surface area, an anatase–rutile mixed phase, and lower bandgap values. Specifically, TiO<inf>2</inf> synthesized at a calcination temperature of 500 °C (HT50) exhibited the highest activity for silver recovery from industrial cyanide-based plating effluent. Approximately 94.13 % of silver ions were recovered within 20 min under UV light irradiation, in the presence of 3.0 vol% ethanol as a hole scavenger and a catalyst loading of 1.5 g/L. This superior performance is likely due to the optimal content of anatase-brookite polymorphs. Besides, HT50 maintained consistent activity over four consecutive uses. The spent TiO<inf>2</inf>, found in the form of Ag/TiO<inf>2</inf>, also exhibited excellent photocatalytic activity for H<inf>2</inf> production under UV light irradiation. The results obtained from this study highlight a strategy for tuning the intrinsic properties of TiO<inf>2</inf> photocatalysts for photocatalytic precious metal recovery, as well as for upcycling metal ions from wastewater by depositing them onto the photocatalyst surface, leading to the formation of a new type of metal-doped photocatalyst that can be further applied in sustainable green energy production.Chemical EngineeringChemistryPhysics and AstronomyArticleSCOPUS10.1016/j.colsurfa.2025.1384202-s2.0-10501664928218734359